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Five-membered 2,3-dioxo heterocycles: LIII. Reaction of 3-Aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones with substituted 1,3,3-trimethyl-3,4-dihydroisoquinolines. A new approach to 13-aza analogs of steroids
| Content Provider | Semantic Scholar |
|---|---|
| Author | Racheva, Nadezhda L. Shklyaev, Yu. V. Rozhkova, Yu. S. Maslivets, Andrey N. |
| Copyright Year | 2007 |
| Abstract | Abstract3-Aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones reacted with substituted 1,3,3-trimethyl-3,4-dihydroisoquinolines to give the corresponding 3-aroyl-4-hydroxy-1-(2-hydroxyphenyl)-5′,5′-dimethyl-5′,6′-dihydro-1H-spiro[pyrrole-2,2′-pyrrolo[2,1-a]isoquinoline]-3′,5-diones. 7′,8′-Benzo derivatives of the latter may be regarded as 13-azagonane analogs having a spiro-fused pyrrole ring at C16. |
| Starting Page | 1330 |
| Ending Page | 1333 |
| Page Count | 4 |
| File Format | PDF HTM / HTML |
| DOI | 10.1134/S1070428007090114 |
| Alternate Webpage(s) | https://page-one.springer.com/pdf/preview/10.1134/S1070428007090114 |
| Alternate Webpage(s) | https://doi.org/10.1134/S1070428007090114 |
| Volume Number | 43 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |
